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    It is Clomid that I am thankful to for having a beautiful baby of three months old. My wife and I have been trying hard to get pregnant for more than four years but nothing could help. We even started thinking about adopting a baby when we came across a new medication that we haven't tried yet. It was something like the last chance and we decided to use it. Clomid was a god sent as after the course of treatment Jenny finally became pregnant and eight months later gave birth to our little princess. They two are everything I have in this life and for half of that everything I owe to Clomid. My boyfriend Sam belongs to the kind of men that start losing their hair pretty early. I love him and this doesn't really matter for me whether curly or bald. One of the main reasons is that inspectors from the U. and India have ramped up efforts to make sure that plants in India making the drugs exported to the U. adhere to the strict manufacturing standards and regulations required by the FDA. A spokesman for the FDA confirmed in an e-mail that the agency is stepping up its efforts abroad, including in India. “The problems FDA investigators encounter in India are similar to those seen around the world in manufacturing,” according to an FDA representative. With more and more companies such as Apotex making drugs in other countries, FDA inspectors were spread far too thin. Last year, the Indian government approved adding seven new FDA drug investigators, to bring the total up to 19 U. “What we’ve found is that most Indian firms understand good manufacturing practices and use them, but we’ve seen problems with a few companies," the representative said. For example, in the last year, the FDA has sent warning letters about manufacturing or packaging violations not only to companies with plants in India, but also to companies operating plants in Australia, Austria, Canada, China, Germany, Japan, Ireland, and Spain. In 2012, Congress passed the FDA Safety and Innovation Act, which among other things, requires the agency to inspect foreign facilities that make drugs sold in the U. "That’s why we‘ve chosen to make quality one of our highest priorities this year.” The agency also says that import bans affect only a fraction of the drugs made in India for the U. Common issues include inadequate testing and quality checks, inconsistencies in data collection, and contaminated products. In particular, imports of drugs and medical devices from China increased by nearly fivefold from 2007 to 2013, and the FDA is scrambling to keep up. Our review of FDA import alerts reveals that the agency sanctioned about as many Chinese factories in the last five years as it did those in India. (Under these alerts, products can be stopped from coming into the U. until the importer proves that they comply with relevant laws and regulations.) As in India, the FDA is working with the Chinese government and plans to increase staff—from the current eight U. officers to 27—to conduct timely inspections of more Chinese plants and other tasks. Manufacturing standards are the same for brand-name and generic drugs. In fact, many brand-name drugs are produced overseas as well, often in the same plants as the generic equivalents. For example, in what is probably the largest related series of drug recalls in U. history, according to an analysis by Quarter Watch, a drug safety publication from the nonprofit Institute for Safe Medication Practices, millions of bottles of over-the-counter medications, including Tylenol and Motrin, were yanked from pharmacy shelves beginning in September 2009 by Johnson & Johnson's Mc Neil Consumer Healthcare subsidiary, headquartered in Fort Washington, Pa.

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